
Journal of Medicinal Chemistry p. 189 - 193 (1978)
Update date:2022-08-02
Topics: Synthesis Precursor Intermediate Analogues Chemical modification Broad-Spectrum Activity Functional Groups Sisomicin Gram-negative bacteria
Davies
Mallams
Counelis
Loebenberg
Moss Jr.
Waitz
The discovery of aminoglycoside 66-40C, a novel dimeric, unsaturated imine produced by Micromonospora inyoensis, afforded a versatile intermediate for the synthesis of a variety of sisomicin analogues modified at the 6' position. The conversion of 66-40C into sisomicin, antibiotic G-52, and a series of novel 6'-substituted analogues of sisomicin is described, and the biological activity of the products is discussed.
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